DOI:
10.1055/s-00000071
Seminars in Neurology
LinksClose Window
References
Muchir A, Bonne G, van der Kooi AJ , et al.
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B).
Hum Mol Genet 2000;
9 (9) 1453-1459
Search in:
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.